美国SCILOGEX(赛洛捷克)大容量电动移液器Levo PluS
ACCUSPIN系统-Histopaque 1077产品说明书
Technical BulletinACCUSPIN™ System – Histopaque ® 1077Catalog Numbers A6929, A7054, and A0561Product DescriptionACCUSPIN System-Histopaque -1077products are intended for use in the isolation of lymphocytes and other mononuclear cells. The separation medium, Histopaque-1077, is a sterile-filtered, endotoxin tested solution of polysucrose and sodium diatrizoate, adjusted to a density of 1.077 g/mL. The ACCUSPIN tube is specially designed with two chambers separated by a porous high density polyethylene barrier (frit).Separation of lymphocytes and other mononuclear cells from whole blood and bone marrow using density gradientseparation media is based on a published method.1 Histopaque-1077 is suitable for human lymphocyte antigen (HLA) typing 2 and as the initial isolation step prior toenumeration of T, B, and ‘null’ lymphocytes.3 It may also be employed in the preparation of pure lymphocyte suspensions for cell culture and cytotoxicity assays.4ACCUSPIN System-Histopaque-1077 products consist of radiation sterilized polypropylene tubes fitted with a highdensity polyethylene frit and aseptically filled with Histopaque-1077.Histopaque-1077 is a sterile-filtered solution of polysucrose, 57 g/L, and sodium diatrizoate, 90 g/L.Density: 1.076–1.078 g/mL Endotoxin: 0.3 EU/mL pH: 8.8–9.0ACCUSPIN System-Histopaque-1077Catalog No. A692940 × 3 mLEach tube contains 3 mL ofHistopaque 1077-1 and will separate 3-6 mL of anticoagulated blood Catalog No. A7054 12 × 15 mLCatalog No. A0561100 × 15 mLEach tube contains 15 mL ofHistopaque 1077-1 and will separate 15-30 mL of anticoagulated bloodReagents and Equipment Required but Not ProvidedCentrifuge (swinging bucket rotor)capable of generating 100 to 1,000 g Centrifuge tubes for washing mononuclear cellsIsotonic phosphate buffered saline solution or appropriate cell culture mediumPrecautions and DisclaimerFor R&D use only. Not for drug, household, or other uses. Please consult the Safety Data Sheet for information regarding hazards and safe handling practices.Preparation InstructionsSpecimen Collection - Collect blood in preservative-free anticoagulant (EDTA or heparin) or use defibrinated blood. For best results, blood should be processed within 2 hours.On occasion, it may be necessary to dilute the blood sample 3 to 5-fold, depending on absolute cell numbers. A similar volume of prediluted blood may be used or the blood sample may be diluted directly in upper chamber of the ACCUSPIN tube (seeProcedure, step 3). This is appropriate for specimens with hematocrits above normal.Storage/StabilityStore the products at 2–8 C.Histopaque-1077 has an expiration period of 3 years. Reagent label bears expiration date.ProcedureAnticoagulated blood can be added to the top chamber of the tube without risk of mixing with the Histopaque-1077 in the lowerchamber under the frit. On centrifugation the whole blood migrates through the frit to contact with the Histopaque-1077. The elements of greater density displace a volume of Histopaque-1077 above the frit giving a clear separation of the bloodcomponents. The erythrocytes aggregate and the granulocytes become slightly hypertonic, increasing their sedimentation rate, resulting in pelleting at the bottom of the ACCUSPIN Tube. Lymphocytes and other mononuclear cells, e.g., monocytes, remain at the plasma/Histopaque-1077 interface. This dense band of mononuclear cells may be collected by pouring off the contents of the upper chamber or by means of a pipette. Erythrocyte contamination is avoided due to the barrier between the chambers.Most extraneous platelets are removed by low speed centrifugation during the washing steps.1. Bring desired number of tubes to roomtemperature. If Histopaque-1077 isabove the frit prior to use, centrifuge at 1,000 g for 30 seconds at room temperature.Note: Failure to bring ACCUSPIN System-Histopaque-1077 to room temperature may cause limited recovery of mononuclear cells. 2. Label tube(s).3. Freely pour the blood sample into theupper chamber of each ACCUSPIN System-Histopaque-1077 tube.a. Use 3–6 mL of whole blood withACCUSPIN System-Histopaque-1077 tubes, Catalog No. A6929. b. Use 15–30 mL of whole blood withACCUSPIN System-Histopaque-1077 tubes, Catalog Nos. A7054 or A0561. Note: Use of volumes of prediluted or whole blood other than those recommended may result in decreased recovery.4. Centrifuge at 1,000 g for 10 minutes atroom temperature or centrifuge at 800 g for 15 minutes at roomtemperature. Centrifugation at lower temperatures, such as 4 C, may result in cell clumping and poor recovery.Note: If platelet contamination is a concern, add the mononuclear cells to a 4-20% sucrose gradient that has been layered over Histopaque-1077.Centrifuge at 1,000 × g for 10 minutes at room temperature. The platelets will pellet at the bottom, while themononuclear cells will migrate to the Histopaque-1077 layer.5. After centrifugation, carefully aspiratethe plasma layer with a Pasteur pipette to within 0.5 cm of the opaque interface containing mononuclear cells. Properly dispose of the plasma layer.Note: Failure to remove the excesssupernatant may result in contamination of the mononuclear band with plasma proteins.6. Carefully transfer the opaque interfacewith a Pasteur pipette into a clean conical centrifuge tube.Note: Removal of Histopaque-1077 with the mononuclear band increasesgranulocyte contamination from residual granulocytes, which may remain at the mononuclear interface.7. Wash the cells by adding 10 mL ofisotonic phosphate buffered saline solution or appropriate cell culture medium and mix by gently drawing in and out of a Pasteur pipette. 8. Centrifuge at 250 g for 10 minutes. 9. Aspirate the supernatant and discard. 10. Resuspend cell pellet with 5 mL ofisotonic phosphate buffered saline solution or appropriate cell culture medium and mix by gently drawing in and out of a Pasteur pipette.11. Centrifuge at 250 g for 10 minutes. 12. Repeat steps 9, 10, and 11, discardsupernatant and resuspend cell pellet in 0.5 mL of isotonic phosphate buffered saline solution or appropriate cell culture medium. Erythrocytes and granulocytes should pellet to the bottom of the ACCUSPIN tube. Mononuclear cells should band at the interface between the Histopaque-1077 and the plasma. If observed results vary from expected results, please contact Sigma-Aldrich Technical Service for assistance.References1. Boyum, A., Separation of leukocytesfrom blood and bone marrow. Scand. J. Clin. Lab. Invest ., 21 (Suppl 97), 77 (1968).2. Amos, D.B., and Pool, P., “HLA typing” inManual of Clinical Immunology, Rose, N.R., and Friedman, H., eds., American Society for Microbiology, (Washington, DC: 1976) pp. 797-804.3. Winchester, R.J., and Ross, G., “Methodsfor enumerating lymphocyte populations” in Manual of Clinical Immunology, Rose, N.R., and Friedman, H. eds., American Society for Microbiology, (Washington, DC: 1976) pp. 64-76.4. Thorsby, E., and Bratlie, A., “A rapidmethod for preparation of pure lymphocyte suspensions.”Histocompatibility Testing, Terasaki, P.I., ed., 665-666 (1970).The life science business of Merck operates as MilliporeSigma in the U.S. and Canada.Merck, Sigma-Aldrich, ACCUSPIN, and Histopaque are trademarks of Merck KGaA, Darmstadt, Germany or its affiliates. All other trademarks are the property of their respective owners. Detailed information on trademarks is available via publicly accessible resources.© 2022 Merck KGaA, Darmstadt, Germany and/or its affiliates. All Rights Reserved.NoticeWe provide information and advice to our customers on application technologies and regulatory matters to the best of our knowledge and ability, but without obligation or liability. Existing laws and regulations are to be observed in all cases by our customers. This also applies in respect to any rights of third parties. Our information and advice do not relieve our customers of their own responsibility for checking the suitability of our products for the envisaged purpose.The information in this document is subject to change without notice and should not be construed as a commitment by the manufacturing or selling entity, or an affiliate. We assume no responsibility for any errors that may appear in this document.Contact InformationFor the location of the office nearest you, go to /offices .Technical ServiceVisit the tech service page on our web site at /techservice .Standard WarrantyThe applicable warranty for the products listed in this publication may be found at /terms .A0561 Technical Bulletin Rev 06/2022。
Centricon Plus-70 中心离心器过滤器指南说明书
User GuideCentricon® Plus-70 Centrifugal FilterFor concentration and purification of biological samplesUFC700308 UFC701008UFC703008 UFC710008Product OverviewThe Centricon® Plus-70 centrifugal filter isa disposable, single-use device designedfor rapid processing of aqueous biological solutions in volumes ranging from 15 to 70 mL.It is compatible with swinging-bucketcentrifuges only. The Centricon® Plus-70 devicecan concentrate most 70 mL solutions downto 350 µL in 15–40 minutes.Usage GuidelinesFor best results be sure to followthe guidelines below.Flow RateFlow rate is affected by several parameters, including the membrane nominal molecularweight limit (NMWL), solute molecular weightand concentration, viscosity, centrifugal force,and temperature. For maximum recovery, selecta device with a NMWL approximately three times lower than the molecular weight of your target molecule. Expect longer spin times for starting solutions with over 5% solids. Flow rates at 4 °C are typically 1.5 times slower than those at 25 °C. Viscous solutions, such as 50% glycerine,will take up to five times longer to concentratethan very dilute solutions.PrerinsingCentricon® Plus membranes contain trace amounts of glycerine, used as a humectant. To remove glycerine, fill device with 70 mL of buffer solutionor Milli-Q® water and spin for 5 minutes. To remove all water and buffer, a recovery spin is required.Do not allow the membrane in filter device to dry out once wet. If the device is not being used immediately after prerinsing, leave fluid on the membrane until the device is used.Desalting or Buffer ExchangeConcentrate a 70 mL sample to 350 µL.Discard filtrate and reconstitute the sample backto 70 mL by adding the required volume of buffer. Concentrate again to 350 µL. Repeat this process until the concentration of the contaminating solutes is reduced. Typically, one wash cycle will remove> 95% of the initial salt content; two cycles will remove > 99.9% of the salt.SanitizationTo sanitize the device, rinse the desired components with a 70% ethanol solution. Chemical CompatibilityUse only with biological fluids and aqueous solutions. See your laboratory products cataloguefor more information.Centricon®Plus-70 Components Cap*Cap*Cap*ConcentrateCollection CupSampleFilter CupFiltrateCollection Cup* Cap fits the Concentrate Collection Cup, Sample Filter Cupand Filtrate Collection Cup, as shown.Sample Concentration1. Add solution to sample filter cup (to a maximumof 70 mL); seal with supplied cap. Place samplefilter cup into filtrate collection cup.2. Place Centricon® Plus-70 assemblyin centrifuge bucket.CAUTION: Before proceeding, check centrifuge clearance by manually moving bucket to itsfull-swing position. Counterbalance centrifugewith a second bucket containing a secondCentricon® Plus-70 device and an equal volume of sample or water.3. Spin at up to 3,500 × g until desiredconcentration is achieved. A typical spin timeis 15–40 minutes, depending on solute typeand concentration. See accompanying flow ratecharts for details.NOTE: If the centrifuge vibrates excessively,stop and rebalance it.4. After the concentration step, removeCentricon® Plus-70 device from centrifugeand separate sample filter cup fromfiltrate collection cup. If retaining the filtrate, cap filtrate collectioncup and store as appropriate.NOTE: When pouringsolution out of the filtratecollection cup, ensurethat the ribs insidethe cup do not obstructthe flow of liquid.Concentrate RecoveryIf the amount of concentrate remaining in the sample filter cup is above the top of the filter cores, decant to a suitable container before proceeding. Be sureto combine this concentrate with the concentrate removed in step 4 below.1. Turn the concentrate cup upside down and placeon top of the sample filter cup.2. Carefully invert device, place in centrifuge, andcounterbalance with a similar device. Spin at nomore than 1,000 × g for up to 2 minutes.CAUTION: Higher spin force can resultin sample loss.3. Remove the concentrate cup containing theconcentrated sample from the sample filter cup.Keep the filter cup inverted during this process.4. Remove the sample with a pipette or cap theconcentrate cup and store sample for later use.NOTE: Samples with high starting proteinconcentration may be subject to recoverylosses due to protein crystallization(protein dependent). This results fromthe high throughput and concentration factorsoffered by Centricon® Plus-70 devices.SpecificationsMaximum volume capacity70 mLMinimum finalconcentrate volume350 µLMaximum centrifugal force3,500 × gfor concentration spin1,000 × gfor recovery spinActive membrane surface area19.0 cm2 (2.95 in2)Hold-up volume of membraneand support 75 µLDimensionsDiameter60 mm (2.36 in.)Length121 mm (4.76 in.)Rotor typeSwinging-bucket capableof handling 250 mL bottles.Do not use a fixed angle rotor.Materials of constructionFiltrate Collection Cup PolypropyleneSample Filter Cup PolypropyleneConcentrate Cup PolypropyleneCap PolypropyleneMembrane Ultracel® regenerated celluloseThe life science business of Merck operates as MilliporeSigma in the U.S. and Canada.Merck, Millipore, Centricon, Milli-Q, Ultracel, and Sigma-Aldrich are trademarksof Merck KGaA, Darmstadt, Germany or its affiliates. All other trademarks are the property of their respective owners. Detailed information on trademarks is available via publicly accessible resources.© 2021 Merck KGaA, Darmstadt, Germany and/or its affiliates. All Rights Reserved.Device PerformanceTypical Flow RatesTypical Filtrate Volume vs. Spin Time®Spin Time (min)Spin conditions:3,500 × g, room temperature, 70 mL starting volume. Protein markers used:Cytochrome c for 3K and 10K, BSA for 30K, and IgG for 100K.Typical Concentrate Volume vs. Spin TimeConcentrate volume (mL)Spin time (min)3KDevice10K Device 30K Device 100K Device5–36.034.2–1043.412.1 1.830.61533.80.40.320.22025.60.30.313.430 5.90.20.3 5.8400.4–– 2.5450.3–– 1.1500.2––0.4Spin conditions:3,500 × g, room temperature, 70 mL starting volume. Protein markers used:Cytochrome c for 3K and 10K, BSA for 30K, and IgG for 100K.Typical Concentrate RecoveryMarker/Concentration Device NMWL Spin Time (min)Concentrate Volume (mL)Concentration Factor (x)ConcentrateRecovery (%)Cytochrome c (0.25 mg/mL)3K 400.418287Cytochrome c (0.25 mg/mL)10K 150.416293BSA(1 mg/mL)30K 150.320794IgG(1 mg/mL)100K207.41091Spin conditions:3,500 × g, room temperature, 70 mL starting volume.Ordering InformationPurchase products online at /products .Centricon ® Plus-70 Centrifugal FiltersDescription,NMWL in Kilodaltons (K)Qty/pkCat. No.Centricon ® Plus-70 device, 3K 8UFC700308Centricon ® Plus-70 device, 10K 8UFC701008Centricon ® Plus-70 device, 30K 8UFC703008Centricon ® Plus-70 device, 100K8UFC710008NoticeWe provide information and advice to our customers on application technologies andregulatory matters to the best of our knowledge and ability, but without obligation or liability.Existing laws and regulations are to be observed in all cases by our customers. This also applies in respect to any rights of third parties. Our information and advice do not relieve our customers of their own responsibility for checking the suitability of our products for the envisaged purpose.The information in this document is subject to change without notice and should not be construed as a commitment by themanufacturing or selling entity, or an affiliate. We assume no responsibility for any errors that may appear in this document.Contact InformationFor the location of the office nearest you, go to /offices .Technical AssistanceVisit the tech service page on our web site at /techservice .Standard WarrantyThe applicable warranty for the productslisted in this publication may be found at /terms .。
Rainin瑞宁移液器及吸头产品索引
传统的移液方式，往往造成操作者的 手部疲劳和重复性劳损(RSI)
RAININ®
：
瑞 宁 移 液 器 远 离 手 部 疲 劳
4
在很多实验室，移液操作都是重复性非常高的工作
● 很多研究人员每天移液操作可长达2-4小时
移液操作是一项比较费力的工作4kg
很多研究人员长期受困于手部疲劳的烦恼，这将导致
RAININ®瑞宁常规移液器.................................................................6
单道移液器产品
Pipet-Lite磁辅移液器.............................................. 6 E-Man Hybrid液晶显示手动移液器...................................8 EDP3电动移液器............................................. ...10 EDP1电动移液器................................................12
符 合
具有多种独特功能，提高实验室移液 效率
人
● 实时传感技术
体
● 带LTS (轻触去吸头系统)，符合人体工程学设计
● 节约贵重样品
工
程 学 设 计 的
瑞 宁 手 动 移
实时移液操作 E-Man Hybrid移液器采用实时传感 技术。LCD显示屏实时持续更新活塞 位置，并生成高精度、四位数容量 设置－消除视觉偏差和机械反冲。 实时的移液器信息，可以帮您扩大 移液应用领域、优化移液方案。
常规移液器配件...................................................................... 34 常规移液器技术参数.................................................................. 35
Thermo-Scientific-Finnpipette-F1多道移液器
【产品名称】手动多道移液器【产品品牌】赛默飞ThermoThermo Scientific Finnpipette F1多道移液器规格：外壳设计：外壳为完全光滑的设计，非磨砂的外壳不易沾污物，易清洗。
外壳防护：纳米银生物安全防护材料，移液器外壳整合纳米银材料，本身即可有效地抑制细菌、真菌、霉菌以及其它微生物的生长，无需进行任何形式的灭菌操作。
液量调节装置：所显示的数字后带微量刻度尺，设定移液量有指针指示。
调节时步进为一个刻度且指针只会停止于刻度线上。
放松指靠设计：指靠为弯钩状设计，使用舒适；指靠也可以120º旋转，适左或右手操作。
显示窗：3×1cm大的量程显示窗，便于观察。
活塞：低于50ul量程的移液器为双活塞设计，即PVDF活塞和金属活塞，以确保移液器能将挂壁液体吹出。
ID标签：配有ID标签，包括各3枚预置标签和空白标签，方便区分。
防遗忘锁扣设计：顶部液量调节按钮抬起时可调液量，移液器使用时按钮自动锁定，停止液量调节。
有效预防移液中间的误操作。
颜色标记：色彩靓丽，不同色彩标记不同的量程，易于辨识，可配合同样颜色标记的吸头配合使用。
证书认证：具有ISO9001:2000 和ISO 13485:2003证书，具有CE认证。
校准维修支持:提供网上在线校准软件支持，可在实验室方便快捷地进行校准和维修。
订购Thermo Scientific F1-ClipTip多道移液器规格：联锁卡点设计：创新的连锁卡点设计，一旦装配上专用的ClipTip吸头，则所有通道完全密封，不会出现松脱现象，确保多通道液面平齐。
外壳设计：外壳为完全光滑的设计，非磨砂的外壳不易沾污物，易清洗。
灭菌消毒：上半支纳米银生物安全防护材料，移液器外壳整合纳米银材料，本身即可有效地抑制细菌、真菌、霉菌以及其它微生物的生长，无需进行其他形式的灭菌操作。
下半支可高温高压灭菌。
液量调节装置：所显示的数字后带微量刻度尺，设定移液量有指针指示。
美国SCILOGEX(赛洛捷克)实验室常用设备 MS-PB标准磁力搅拌器
SCILOGEX仪器始终与国际第三方认证机构TÜV德国莱茵公司合作，其全系列产品都经过该公司全面严格的安全检测，获得由该公司颁发的CE、cTUVus、FCC国际通行的安全标准证书。
TÜV德国莱茵公司系最具公信力的欧盟官方指定认证机构(欧盟官方公告号019) 。
MS- PBBlueSpin标准型磁力搅拌器- 转速范围100-1500 rpm- 最大搅拌量3L- 微处理器的反馈控制技术确保转速的精确性- 全封闭阻燃塑料外壳磁力搅拌芯的适用型号(不加热型)磁力搅拌芯和磁力搅拌芯取出器，150℃下永磁适用型号MS7-Pro MS-S MS-PAMS-PBMS-M-S10货号磁力搅拌芯规格[mm]适用最长搅拌芯80mm适用最长搅拌芯50mm适用最长搅拌芯40mm18900006 10mm x 6mm ●●●18900007 15mm x 8mm ●●●18900008 20mm x 8mm ●●●18900009 25mm x 8mm ●●●12500005 30mm x 6m ●●●18900011 40mm x 8mm ●●●12500004 51mm x 8mm ●●18900013 65mm x 8mm ●18900014 80mm x 13mm ●18900015 搅拌芯取出器，长度20cm●●●磁力搅拌器订货信息货号型号产品描述813213010000MS7-Pro BlueSpin LCD数控型7寸方盘磁力搅拌器，玻璃陶瓷盘面，国标插头，220V/50Hz/60Hz811111010000 MS-S BlueSpin标准型磁力搅拌器，不锈钢盘面，国标插头，110V/220V/50Hz/60Hz811111110000 MS-S BlueSpin标准型磁力搅拌器，陶瓷涂层盘面，国标插头，110V/220V/50Hz/60Hz861521130000 MS-PA BlueSpin LED数显型圆盘磁力搅拌器，塑料盘面，国标插头，100-240V/50Hz/60Hz861520130000 MS-PB BlueSpin标准型圆盘磁力搅拌器，塑料盘面，国标插头，100-240V/50Hz/60Hz811311010000 MS-M-S10 BlueSpin 10通道标准型磁力搅拌器，国标插头，110V/220V/50Hz/60Hz。
移液器的分类和原理
移液器的分类和原理微量加样器（移液器）最早出现于1956年，由德国生理化学研究所的科学家Schnitger发明，其后，在1958年德国Eppendorf公司开始生产按钮式微量加样器，成为世界上第一家生产微量加样器的公司。
这些微量加样器的吸液范围在1—1000~1之间，适用于临床常规化学实验室使用。
微量加样器发展到今天，不但加样更为精确，而且品种也多种多样，如微量分配器、多通道微量加样器等，其加样的物理学原理有下面两种：①使用空气垫(又称活塞冲程)加样；②使用无空气垫的活塞正移动(positive displacement)加样。
上述两种不同原理的微量加样器有其不同的特定应用范围。
空气垫加样器活塞冲程(空气垫)加样器可很方便地用于固定或可调体积液体的加样，加样体积的范围在小于1ul至lOml之间。
加样器中的空气垫的作用是将吸于塑料吸头内的液体样本与加样器内的活塞分隔开来，空气垫通过加样器活塞的弹簧样运动而移动，进而带动吸头中的液体，死体积和移液吸头中高度的增加决定了加样中这种空气垫的膨胀程度。
因此，活塞移动的体积必须比所希望吸取的体积要大约2％～4％，温度、气压和空气湿度的影响必须通过对空气垫加样器进行结构上的改良而降低，使得在正常情况下不至于影响加样的准确度。
一次性吸头是本加样系统的一个重要组成部分，其形状、材料特性及与加样器的吻合程度均对加样的准确度有很大的影响。
活塞正移动加样器以活塞正移动为原理的加样器和分配器与空气垫加样器所受物理因素的影响不同，因此，在空气垫加样器难以应用的情况下，活塞正移动加样器可以应用，如具有高蒸汽压的、高黏稠度以及密度大于2．0g ／cm3的液体；又如在临床聚合酶链反应(PCR)测定中，为防止气溶胶的产生，最好使用活塞正移动加样器。
活塞正移动加样器的吸头与空气垫加样器吸头有所不同，其内含一个可与加样器的活塞耦合的活塞，这种吸头一般由生产活塞正移动加样器的厂家配套生产，不能使用通常的吸头或不同厂家的吸头。
美国SCILOGEX(赛洛捷克)实验室常用设备 旋转混匀仪MX-RL-Pro MX-RD-Pro
旋转混匀仪MX-RL-Pro / MX-RD-Pro旋转混匀仪可充分混合微量管内的样品和制备样品时的预处理，容量范围1.5-50ml 。
可调转速和旋转角度。
适用于预防血液凝固、乳胶诊断、免疫沉淀等相似应用。
NewLCD显示屏可同时显示速度和定时时间☑ 速度范围：10 - 70rpm ☑ 可调混合角度：0 - 90o ☑ 多种离心管夹具可选，适用1.5-50ml 微量管 ☑ 定时和连续运转两种模式 MX-RD-Pro 主机 LCD 数控旋转混匀仪 主机 + 单个圆盘离心管夹具 3个规格任选 主机 + 两个圆盘离心管夹具 + 圆盘加层连接杆技术指标MX-RD-Pro / MX-RL-Pro 电压 [VAC] 100-240 频率 [Hz] 50/60 功率 [W] 40 电机 直流电机 角度 [o ] 0-90 速度范围 [rpm] 10-70 速度显示 LCD 定时 Yes 时间显示LCD 时间设置范围 [min] 1-1199 运行方式定时/连续运转 尺寸 [D×W×H mm] 510×190×260 重量 [kg]8 允许环境温度范围 [℃] 5-40 允许相对湿度80% DIN EN60529保护方式IP21MX-RL-Pro 主机 LCD 数控旋转混匀仪 主机 + 长轴离心管夹具 6个规格任选附件货号：18900137 适用于MX-RD-Pro 圆盘离心管夹具，1.5ml x 60 离心管 货号：18900138 适用于MX-RD-Pro 圆盘离心管夹具，15ml x 16 离心管货号：18900139 适用于MX-RD-Pro 圆盘离心管夹具，50ml x 8 离心管货号：18900140 适用于MX-RD-Pro圆盘加层连接杆，4根货号：18900142 适用于MX-RL-Pro 长轴离心管夹具，可水平安装1.5ml x 48 离心管 货号：18900143 适用于MX-RL-Pro 长轴离心管夹具，可水平安装15ml x 24 离心管货号：18900144 适用于MX-RL-Pro 长轴离心管夹具，可水平安装50ml x 24 离心管 货号：18900145 适用于MX-RL-Pro 长轴离心管夹具，可竖直安装1.5ml x 32 离心管货号：18900146适用于MX-RL-Pro长轴离心管夹具，可竖直安装15ml x 16 离心管货号：18900147 适用于MX-RL-Pro 长轴离心管夹具，可竖直安装50ml x 16 离心管订货信息主机订货号型号描述824232110000 MX-RD-Pro LCD数控旋转混匀仪(不含离心管夹具), 可调速，110V-240V/50HZ/60HZ，国标插头824222110000 MX-RL-Pro LCD数控旋转混匀仪(不含离心管夹具), 可调速，110V-240V/50HZ/60HZ，国标插头。
RAININ移液器产品目录
量程 0.1μl–2μl 0.5μl–10μl 2μl–20μl 10μl–100μl 20μl–200μl 20μl–300μl 100μl–1000μl 200μl–2000μl 500μl–5000μl 1ml–10ml 移液器套装 SL-START
订货号 17003606 17003609 17003619 17003613 17003622 17007313 17003616 17003624 17003626 17003611 17006694
● 手部重复性劳损(RSI) ● 移液准确性降低 ● 移液操作效率降低
什么原因导致了较大的移液活塞推进力？
传统的移液活塞推进力 4kg
1
2
什么原因导致了退吸头所用的较大手腕力？
传统移液器退吸头所需的手腕力 4kg
1 2
1 吸液弹簧 慢慢压下吸液弹簧， 直到第一个停顿点
2 排液弹簧 下压弹簧到第一个停 顿点，然后继续用力 下压弹簧到第二停顿 点，将液体完全排 出。
LTS多道移液器产品
LTS多道移液器概述.............................................. 14 Pipet-Lite LTS磁辅手动多道移液器..................................16 EDP3-Plus LTS电动多道移液器.....................................17 Pipet-Lite间距可调手动多道移液器................................. 18 EDP3-间距可调电动多道移液器................................... 19
3
传统的移液方式，往往造成操作者的 手部疲劳和重复性劳损(RSI)
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美国SCILOGEX （赛洛捷克）大容量电动移液器Levo PluS
【产品简介】
LevoPlus 大容量电动移液器 轻质、无线、人机工效学的设计使移液操作简单、高效，单手轻松控制。
能满足您不同环境的实验需求。
【详细说明】
大屏幕液晶屏显示8个速度设置和电量信息
轻触调速器按钮，可便捷地调整吸液和分液的速度
指尖控制吸液和分液速度，保了移液的准确性
量程范围广0.1-100ml
轻质、无线、人机工效学的设计使移液操作简单、高效，单手轻松控制
通过电路反馈自动调节吸液和分液的速度
可更换的锂电池使用时间长，无记忆效应
有电力不足时警告功能
大功率马达可快速充满100ml 液体
LevoPlus 大容量电动移液器技术参数：。